MAS1862

GUDID 20888551042458

ADHESIVE SENSOR LNCS NEO-L

STERILMED, INC.

Pulse oximeter probe, reprocessed
Primary Device ID20888551042458
NIH Device Record Keyfb52588c-5048-4548-92f2-aac3c8390efb
Commercial Distribution Discontinuation2019-04-17
Commercial Distribution StatusNot in Commercial Distribution
Version Model NumberMAS1862
Catalog NumberMAS1862
Company DUNS175899459
Company NameSTERILMED, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110888551042451 [Primary]
GS120888551042458 [Package]
Contains: 10888551042451
Package: Carton [24 Units]
Discontinued: 2019-04-17
Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NLFOXIMETER, REPROCESSED

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


[20888551042458]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-04-17
Device Publish Date2016-09-22

Devices Manufactured by STERILMED, INC.

10888551045179 - NA2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, F CURVE
10888551045186 - NA2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, D CURVE
10888551045193 - NA2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, F CURVE
10888551045209 - NA2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, D CURVE
10888551010313 - NA2021-01-22 KNIFE SET ECTRA II (PACK OF 3)
10888551021531 - NA2021-01-22 KNIVES (1) HOOK BLADE (1) TRIANGLE BLADE ENDOTRAC BLADE SYSTEM
10888551000048 - NA2020-11-06 CTS RELIEF KIT, 5PC SET
10888551012928 - NA2020-10-19 ENDO LUNG

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